Okada Masahiko, Ohgino Keiko, Horiuchi Kohei, Sayama Koichi, Arai Daisuke, Watase Mayuko, Kobayashi Keigo, Terashima Takeshi, Ishioka Kota, Miyawaki Masayoshi, Sakamaki Fumio, Masuzawa Keita, Terai Hideki, Yasuda Hiroyuki, Soejima Kenzo, Fukunaga Koichi
Division of Pulmonary Medicine, Department of Medicine, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku 160-0016, Tokyo, Japan.
Icahn School of Medicine at Mount Sinai, Mount Sinai Morningside and West, 1000 Tenth Avenue, New York, NY 10019, USA.
J Clin Med. 2024 Dec 20;13(24):7815. doi: 10.3390/jcm13247815.
Atezolizumab, an immune checkpoint inhibitor (ICI), was used in a phase III clinical trial, i.e., the OAK trial, of previously treated patients with non-small cell lung cancer. We aimed to evaluate the real-world efficacy and safety of atezolizumab in a non-selected population and identify the clinical characteristics that influence its efficacy. This was a multicenter, retrospective, single-arm observational study. Seventy-four patients with advanced non-small cell lung cancer, who received atezolizumab monotherapy at Keio University and affiliated hospitals in Japan between April 2018 and March 2019, were enrolled. The follow-up period was until 28 February 2024. The efficacy of treatment and adverse events were reviewed retrospectively. Statistical analyses using Pearson's χ test, Fisher's exact test, log-rank test, and Student's -test were performed. The median age of patients was 70 (range, 45-85) years. The overall survival duration was 7.54 (95% confidence interval [CI], 5.14-11.3) months, and the median time to treatment failure (TTF) was 2.00 (95% CI, 1.75-2.54) months. Patients treated with atezolizumab as their first ICI had a longer TTF than those treated with atezolizumab as their second or subsequent ICI ( = 0.04). Atezolizumab may be more effective when used as the first ICI for previously treated patients and may be safely used in elderly patients with non-small cell lung cancer in real-world settings.
阿替利珠单抗是一种免疫检查点抑制剂(ICI),曾用于一项针对既往接受过治疗的非小细胞肺癌患者的III期临床试验,即OAK试验。我们旨在评估阿替利珠单抗在非选择性人群中的真实疗效和安全性,并确定影响其疗效的临床特征。这是一项多中心、回顾性、单臂观察性研究。纳入了2018年4月至2019年3月期间在日本庆应义塾大学及其附属医院接受阿替利珠单抗单药治疗的74例晚期非小细胞肺癌患者。随访期至2024年2月28日。对治疗疗效和不良事件进行回顾性分析。采用Pearson卡方检验、Fisher精确检验、对数秩检验和Student t检验进行统计分析。患者的中位年龄为70岁(范围45 - 85岁)。总生存时长为7.54个月(95%置信区间[CI],5.14 - 11.3),中位治疗失败时间(TTF)为2.00个月(95% CI,1.75 - 2.54)。将阿替利珠单抗作为首个ICI治疗的患者的TTF长于将其作为第二个或后续ICI治疗的患者(P = 0.04)。对于既往接受过治疗的患者,将阿替利珠单抗作为首个ICI使用时可能更有效,且在真实世界环境中可安全用于老年非小细胞肺癌患者。